Educational Discharge Video Impact on Post-Operative Healthcare Utilization After HoLEP
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
Age18+
SponsorUniversity of California, San Francisco
About this trial
This will be a randomized interventional study. Patients scheduled to undergo a HoLEP at UCSF will be randomized into two groups after the procedure: one group will watch a scripted educational HoLEP video and the other group will not receive a video. We will monitor the post-operative care utilization after discharge. Secondary outcomes will include patient satisfaction.
Eligibility criteria
Qualifiers
Adults aged 18+
Patients scheduled for a HoLEP procedure
Patients willing to complete both baseline and follow up surveys
Patients able to provide informed consent
Disqualifiers
Patients under 18+
Patients unable to consent
Patients unable to complete surveys
Patients without a prostate.
Trial design
Treatments tested in this trial
- Video
Treatment groups
114 Participants
are divided into 2 treatment groupsLocations
3University of California, San Francisco94143, San FranciscoCalifornia, United States
University of Rochester Medical Center14620, RochesterNew York, United States
Scott SUNY Upstate Medical University13210, SyracuseNew York, United States
Sponsors and collaborators
University of California, San Francisco
Lead sponsor
State University of New York - Upstate Medical University
Collaborator
University of Rochester
Collaborator
Source ClinicalTrials.gov